EP0121875A2 - Procédé de production de teintures et d'impressions rongeables en milieu alcalin - Google Patents

Procédé de production de teintures et d'impressions rongeables en milieu alcalin Download PDF

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Publication number
EP0121875A2
EP0121875A2 EP84103518A EP84103518A EP0121875A2 EP 0121875 A2 EP0121875 A2 EP 0121875A2 EP 84103518 A EP84103518 A EP 84103518A EP 84103518 A EP84103518 A EP 84103518A EP 0121875 A2 EP0121875 A2 EP 0121875A2
Authority
EP
European Patent Office
Prior art keywords
methyl
ethyl
methoxy
chlorine
hydrogen
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP84103518A
Other languages
German (de)
English (en)
Other versions
EP0121875A3 (fr
Inventor
Udo Dr. Bergmann
Johannes Peter Dr. Dix
Guenter Dr. Hansen
Hans Weber
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by BASF SE filed Critical BASF SE
Publication of EP0121875A2 publication Critical patent/EP0121875A2/fr
Publication of EP0121875A3 publication Critical patent/EP0121875A3/fr
Withdrawn legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B29/00—Monoazo dyes prepared by diazotising and coupling
    • C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
    • C09B29/08—Amino benzenes
    • C09B29/0805—Amino benzenes free of acid groups
    • C09B29/0807—Amino benzenes free of acid groups characterised by the amino group
    • C09B29/0809—Amino benzenes free of acid groups characterised by the amino group substituted amino group
    • C09B29/0811—Amino benzenes free of acid groups characterised by the amino group substituted amino group further substituted alkylamino, alkenylamino, alkynylamino, cycloalkylamino aralkylamino or arylamino
    • C09B29/0815—Amino benzenes free of acid groups characterised by the amino group substituted amino group further substituted alkylamino, alkenylamino, alkynylamino, cycloalkylamino aralkylamino or arylamino substituted by -C(=O)-
    • C09B29/0816—Amino benzenes free of acid groups characterised by the amino group substituted amino group further substituted alkylamino, alkenylamino, alkynylamino, cycloalkylamino aralkylamino or arylamino substituted by -C(=O)- substituted by -COOR
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P5/00—Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
    • D06P5/15—Locally discharging the dyes
    • D06P5/17—Azo dyes

Definitions

  • Alkylene radicals A are e.g. B .: in particular and preferably -C 2 H 4 -.
  • C-Acylamino radicals R 4 correspond to the formula NHCO R 5 , where R 5 z.
  • B C 1 - to C 6 -alkyl, which is also substituted by hydroxy, chlorine, bromine, methoxy, ethoxy, cyano, C 1 - to C 4 -alkoxyethoxy, C 1 - to C 4 -alkoxymethylethoxy, C 1 - to C 4 Alkoxyethylethoxy, phenoxy, C 1 -C 6 -alkoxycarbonyloxy, C 1 - to C6-alkylaminocarbonyloxy, phenylaminocarbonyloxy or C 1 - to C 6 -alkanoyloxy may be substituted, cyclohexyl, furfuryl, tetrahydrofurfuryl, allyl, methallyl, benzyl, phenethyl or optionally phenyl substituted by chlorine, bromine, methyl,
  • R 5 are in addition to the z. E.g .: methyl, ethyl, propyl, butyl, pentyl, hexyl, hydroxyethyl, chloroethyl, bromoethyl, cyanomethyl, methoxymethyl, phenyl, o-, m-, p-tolyl, o-, m-, p-methoxyphenyl, o-, m-, p-chlorophenyl or o-, m-, p-nitrophenyl.
  • R 1 and R 2 are the same radicals in the general definition may be mentioned for R 5, R 1 moreover by C 1 - to C 6 alkoxycarbonyl-substituted C I - or C 2 -alkyl, z.
  • B methoxycarbonylethyl, ethoxycarbonylethyl, n- or i-propoxycarbonylethyl, n- or i-butoxycarbonylethyl, methoxycarbonylmethyl or ethoxycarbonylmethyl.
  • the dyes are prepared as usual by methods known per se.
  • a padding liquor which contains 930 parts of water, 10 parts of monosodium phosphate, 10 parts of sodium chlorate and 10 parts of a polyacrylic acid-based polymerization product.
  • a polyester fabric is prepared with this padding liquor on a padder and dried at 110 ° C.
  • the fabric is then printed on a flat film printing machine with a printing paste which contains 300 parts of a 10% strength aqueous core meal ether thickener, 300 parts of a starch ether strengthening (10% strength), 100 parts of polyethylene glycol (molecular weight 300), 80 parts of potash and 220 parts of water.
  • the result is a dark blue print with good fastness properties, which has white ' sharp-edged patterns at the areas pre-printed with the sodium hydroxide-containing paste.
  • a padding liquor which contains 940 parts of water, 5 parts of monosodium phosphate, 10 parts of sodium chlorate and 15 parts of a polymerization product based on acrylic acid as an anti-migration agent.
  • a printing paste containing 400 parts of an aqueous 10% strength meal ether thickener, 200 parts of an aqueous 10% strength starch thickener, 150 parts of water glass, 50 parts of glycerol, 50 parts of polyethylene glycol (molecular weight 300) and 150 parts of water.
  • alkali can also be used to produce white-etchable prints with very good coloristic properties if the dyes identified in the table below are used.

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)
  • Detergent Compositions (AREA)
EP84103518A 1983-04-07 1984-03-30 Procédé de production de teintures et d'impressions rongeables en milieu alcalin Withdrawn EP0121875A3 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19833312488 DE3312488A1 (de) 1983-04-07 1983-04-07 Verfahren zur herstellung alkalisch aetzbarer faerbungen und drucke
DE3312488 1983-04-07

Publications (2)

Publication Number Publication Date
EP0121875A2 true EP0121875A2 (fr) 1984-10-17
EP0121875A3 EP0121875A3 (fr) 1984-12-19

Family

ID=6195665

Family Applications (1)

Application Number Title Priority Date Filing Date
EP84103518A Withdrawn EP0121875A3 (fr) 1983-04-07 1984-03-30 Procédé de production de teintures et d'impressions rongeables en milieu alcalin

Country Status (3)

Country Link
EP (1) EP0121875A3 (fr)
JP (1) JPS59204989A (fr)
DE (1) DE3312488A1 (fr)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0148433A1 (fr) * 1983-12-15 1985-07-17 BASF Aktiengesellschaft Procédé pour la préparation d'impressions par gravure
EP0151287A2 (fr) * 1984-01-07 1985-08-14 BASF Aktiengesellschaft Colorants azoiques de la série isothiazole
EP0293745A2 (fr) * 1987-06-03 1988-12-07 BASF Aktiengesellschaft Procédé pour la préparation de gravures à l'eau forte
US5723587A (en) * 1993-05-06 1998-03-03 Ciba Specialty Chemicals Corporation Azo dyes

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2028383A (en) * 1978-08-19 1980-03-05 Cassella Ag Process for dyeing and printing synthetic hydrophobic fibre material
EP0013378A1 (fr) * 1978-12-27 1980-07-23 CASSELLA Aktiengesellschaft Procédé pour la réalisation d'effets de réserve sur des matières textiles fibreuses mixtes polyester-cellulose
EP0036252A2 (fr) * 1980-03-13 1981-09-23 Imperial Chemical Industries Plc Procédé d'impression de textiles
EP0051261A1 (fr) * 1980-10-31 1982-05-12 CASSELLA Aktiengesellschaft Procédé pour réaliser des impressions au rongeant-réserve sur des matières textiles
JPS5787463A (en) * 1980-11-20 1982-05-31 Nippon Kayaku Co Ltd Azo compound, dyeing and printing of synthetic fibers using it

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2028383A (en) * 1978-08-19 1980-03-05 Cassella Ag Process for dyeing and printing synthetic hydrophobic fibre material
EP0013378A1 (fr) * 1978-12-27 1980-07-23 CASSELLA Aktiengesellschaft Procédé pour la réalisation d'effets de réserve sur des matières textiles fibreuses mixtes polyester-cellulose
EP0036252A2 (fr) * 1980-03-13 1981-09-23 Imperial Chemical Industries Plc Procédé d'impression de textiles
EP0051261A1 (fr) * 1980-10-31 1982-05-12 CASSELLA Aktiengesellschaft Procédé pour réaliser des impressions au rongeant-réserve sur des matières textiles
JPS5787463A (en) * 1980-11-20 1982-05-31 Nippon Kayaku Co Ltd Azo compound, dyeing and printing of synthetic fibers using it

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
CHEMICAL ABSTRACTS, Band 97, Nr. 26, 27. Dezember 1982, Seite 101, Nr. 218021g, Columbus, Ohio, US; & JP - A - 82 87 463 NIPPON KAYAKU CO., LTD.) 31-05-1982 *
RESEARCH DISCLOSURE, Band 198, Oktober 1980, Seiten 425-427, Nr. 19826, Havant, Hampshire, GB; "Discharge/resist printing of synthetic textile materials using thiophene-azo disperse dyestuffs in the presence of alkali" *

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0148433A1 (fr) * 1983-12-15 1985-07-17 BASF Aktiengesellschaft Procédé pour la préparation d'impressions par gravure
EP0151287A2 (fr) * 1984-01-07 1985-08-14 BASF Aktiengesellschaft Colorants azoiques de la série isothiazole
EP0151287A3 (en) * 1984-01-07 1985-09-25 Basf Aktiengesellschaft Isothiazole azodyes
EP0293745A2 (fr) * 1987-06-03 1988-12-07 BASF Aktiengesellschaft Procédé pour la préparation de gravures à l'eau forte
EP0293745A3 (fr) * 1987-06-03 1991-08-14 BASF Aktiengesellschaft Procédé pour la préparation de gravures à l'eau forte
US5723587A (en) * 1993-05-06 1998-03-03 Ciba Specialty Chemicals Corporation Azo dyes
CN1059456C (zh) * 1993-05-06 2000-12-13 希巴特殊化学控股公司 偶氮染料及其制法和用途

Also Published As

Publication number Publication date
JPS59204989A (ja) 1984-11-20
EP0121875A3 (fr) 1984-12-19
DE3312488A1 (de) 1984-10-11

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Inventor name: DIX, JOHANNES PETER, DR.

Inventor name: WEBER, HANS

Inventor name: BERGMANN, UDO, DR.

Inventor name: HANSEN, GUENTER, DR.